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Results 1 - 10 of 34 for Syndromic genetic hearing loss
  1. Bart-Pumphrey syndrome is characterized by nail and skin abnormalities and hearing loss.People with Bart-Pumphrey syndrome typically have a white discoloration ...
  2. Palmoplantar keratoderma with deafness is a disorder characterized by skin abnormalities and hearing loss. Affected individuals develop unusually thick skin on the ...
  3. Keratitis-ichthyosis-deafness (KID) syndrome is characterized by eye problems, skin abnormalities, and hearing loss.People with KID syndrome usually have keratitis, ...
  4. Vohwinkel syndrome is a disorder with classic and variant forms, both of which affect the skin.In the classic form of Vohwinkel syndrome, affected individuals ...
  5. Hystrix-like ichthyosis with deafness (HID) is a disorder characterized by dry, scaly skin (ichthyosis) and hearing loss that is usually profound. Hystrix-like ...
  6. Hearing and Balance Symptoms and Conditions (American Academy of Audiology)  
    Hearing Disorders and Deafness/Specifics ... Hearing Disorders and Deafness ... American Academy of Audiology ... Hearing and balance symptoms could be identifiers for ...
  7. Enlarged Vestibular Aqueduct (EVA) (Vestibular Disorders Association)  
    Enlarged Vestibular Aqueduct is a condition caused by a malformation in the inner ear that leads to loss of hearing and vestibular function. ... Dizziness ...
  8. ... cell is sufficient to cause the disorder. JWS ... Agochukwu NB, Solomon BD, Muenke M. Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings. Int J ...
  9. ... described as syndromic. The most common form of syndromic retinitis ... genetic syndromes, including Bardet-Biedl syndrome; Refsum disease; and ...
  10. ... associated with nonsyndromic hearing loss can also cause syndromic forms of ... to genetic changes, hearing loss can result from environmental factors ...
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